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Results 1 - 7 of 7 for Cone dystrophy "1," "X-linked"
  1. ... LINKED, 3; CORDX3 CONE-ROD DYSTROPHY 6; CORD6 CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 CONE-ROD DYSTROPHY 5; CORD5 CONE-ROD DYSTROPHY, X-LINKED, 2; CORDX2 CONE-ROD DYSTROPHY 7; CORD7 CONE- ...
  2. ... WITHOUT DEAFNESS; RPSRDF RETINITIS PIGMENTOSA GTPase REGULATOR; RPGR CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 NCBI Gene ClinVar Ayyagari R, Demirci FY, ...
  3. ... J, Sankila EM, Alitalo T, Bech-Hansen NT. X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the ...
  4. ... conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch syndrome, and Cohen ...
  5. ... present in other family members. Pigmentary retinopathy Rod-cone dystrophy RP Tapetoretinal degeneration Genetic Testing Registry: Retinitis pigmentosa ...
  6. ... OPN1SW Red-green color vision defects and blue cone monochromacy are inherited in an X-linked recessive pattern. The OPN1LW and OPN1MW genes are ... TR, Mollon JD, Moore AT, Hardcastle AJ. Blue cone monochromacy: causative mutations and ... Epub 2009 May 1. Citation on PubMed or Free article on PubMed ...
  7. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    muscular dystrophy; exercise with a disability; neuromuscular disease; adapted exercise; accesible sports equipment; power wheelchair; power soccer